934601-94-2

Upstream product

• 934601-93-1 tert-butyl 3-(2-iodophenyl)propanoate 
• 2028-63-9 but-3-yn-2-ol 
• 26260-02-6 2-iodobenzaldehyde 
• 96606-95-0 3-(2-iodophenyl)propanoic acid 

Downstream Products

• 934601-95-3 tert-butyl 3-(2-(3-oxobut-1-ynyl)phenyl)propanoate 
• 1269806-77-0 pentane-1,5-diyl bis(3-(2-(3-oxobut-1-ynyl)phenyl)propanoate) 
• 1269806-78-1 hexane-1,6-diyl bis(3-(2-(3-oxobut-1-ynyl)phenyl)propanoate) 
• 1269806-79-2 2,2'-oxybis(ethane-2,1-diyl) bis(3-(2-(3-oxobut-1-ynyl)phenyl)propanoate) 
• 1269806-80-5 2,2'-(ethane-1,2-diylbis(oxy))bis(ethane-2,1-diyl) bis(3-(2-(3-oxobut-1-ynyl)phenyl)propanoate) 
• 1269806-81-6 3-(2-(3-oxobut-1-ynyl)phenyl)propanoic acid 
• 934601-96-4 C₁₄H₁₄O₃ 

Relevant academic research and scientific papers

Preparation of strained axially chiral (1,5)naphthalenophanes by photo-dehydro-diels-Alder reaction

The preparation of 10 (1,5)naphthalenophanes (10a-j) by photo-dehydro-Diels-Alder (PDDA) reaction is described. Owing to hindered rotation around the biaryl axis, compounds 10 are axially chiral and the separation of enantiomers by chiral HPLC was demonst

The Photo-Dehydro-Diels-Alder (PDDA) reaction - A powerful method for the preparation of biaryls

The photochemically initiated dehydro-Diels-Alder (PDDA) reaction is an efficient and versatile method for the preparation of biaryls. The ring closure may take place both inter- and intramolecularly, of which the intramolecular variant is more productive